P
US8636711B2ActiveUtilityPatentIndex 51

Stabilized glucagon solutions and uses therefor

Assignee: WARD W KENNETHPriority: Jun 14, 2010Filed: Jun 14, 2011Granted: Jan 28, 2014
Est. expiryJun 14, 2030(~3.9 yrs left)· nominal 20-yr term from priority
Inventors:WARD W KENNETHDIMARCHI RICHARD D
A61K 47/183A61M 5/145A61K 38/26A61P 3/10A61K 9/0019A61K 9/08A61M 5/1723
51
PatentIndex Score
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Cited by
96
References
20
Claims

Abstract

Stabilized glucagon solutions, methods of storing and using the stabilized glucagon solutions, and drug delivery devices containing the stabilized glucagon solutions. In some embodiments, the glucagon solutions may be alkaline, such as with a pH of at least about 9. The glucagon solutions may be resistant to aggregation of glucagon when the solutions are stored for a prolonged period, such as at least about three days, at room temperature and/or physiological temperature.

Claims

exact text as granted — not AI-modified
The invention claimed is: 
     
       1. A method of treating a glucagon-responsive medical condition, comprising:
 providing an aqueous solution of glucagon at a pH of greater than about 9; 
 storing the solution in liquid form at a pH of greater than about 9 for at least three days at room temperature or higher without substantial aggregation of the glucagon; and 
 delivering at least a portion of the solution into a subject after the step of storing. 
 
     
     
       2. The method of  claim 1 , wherein the glucagon is present at a concentration of at least about 0.5 mg/mL. 
     
     
       3. The method of  claim 1 , wherein the solution is stored at a pH of about 9.5 to 10.5. 
     
     
       4. The method of  claim 1 , wherein the solution includes a buffering agent comprising an ampholyte. 
     
     
       5. The method of  claim 4 , wherein the ampholyte is glycine. 
     
     
       6. The method of  claim 1 , wherein the solution is substantially free of detergent. 
     
     
       7. The method of  claim 1 , wherein the step of storing is performed in a drug delivery device, and wherein the step of delivering is performed with the drug delivery device. 
     
     
       8. The method of  claim 1 , wherein the step of delivering is performed by injection intravenously, intramuscularly, or subcutaneously. 
     
     
       9. The method of  claim 1 , wherein the subject is hypoglycemic. 
     
     
       10. The method of  claim 1 , wherein the step of delivering is controlled by a processor that is in communication with at least one glucose sensor that monitors glucose concentration of the subject. 
     
     
       11. The method of  claim 10 , wherein the processor is programmed to cause delivery of the solution based on a proportional error and/or a derivative error of the glucose concentration. 
     
     
       12. The method of  claim 11 , wherein the timing and amount of glucagon delivered is based on the proportional error and the derivative error. 
     
     
       13. The method of  claim 11 , wherein the processor is programmed to use a fading memory proportional derivative algorithm to determine the timing and amount of glucagon delivered, based on a signal from the at least one glucose sensor. 
     
     
       14. A drug delivery system, comprising:
 a drug delivery device including a container holding an aqueous solution of glucagon that has been stored in the container at a pH of greater than about 9 and at room temperature or higher for at least three days, the glucagon being substantially non-aggregated, the device also including an outlet through which the solution is configured to be driven from the container for delivery into a subject. 
 
     
     
       15. The drug delivery system of  claim 14 , further comprising a pressure source operatively disposed to drive the solution from the container through the outlet. 
     
     
       16. The drug delivery system of  claim 15 , further comprising at least one glucose sensor and a processor programmed to control operation of the pressure source based on a signal received from the glucose sensor. 
     
     
       17. The drug delivery system of  claim 16 , wherein the processor is programmed to control operation of the pressure source based on a proportional error and/or a derivative error of glucose concentration measured by the glucose sensor. 
     
     
       18. The drug delivery system of  claim 17 , wherein the processor is programmed to control the timing and amount of glucagon delivered based on the proportional error and the derivative error. 
     
     
       19. The method of  claim 1 , wherein the step of storing is performed at a pH of greater than about 9 for at least three days at a physiological temperature. 
     
     
       20. The system of  claim 14 , wherein the solution of glucagon has been stored in the container at a pH of greater than about 9 for at least three days at a physiological temperature.

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